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Access multiple gene data backends through one searchable unified MCP endpoint.
Copy the install command and let the AI configure it · recommended for beginners
No copy-paste install info for "genefoundry" yet — see the docs or source repo.
List the available tools in genefoundry related to gene expression, variant annotation, and population frequency, and explain the best research use case for each.
A categorized list of tools with brief descriptions of their purpose and ideal research scenarios.
Query a gene across genefoundry-accessible sources for variant information, population frequency, and GTEx expression summaries, then compile the results into a comparison table.
An integrated comparison table summarizing key variants and expression data across sources.
I am building a genetics analysis workflow. Based on the backends discoverable in genefoundry, recommend a tool combination for variant filtering, functional interpretation, and tissue-expression validation.
A step-by-step tool recommendation plan explaining why each backend fits that stage.
Access, search, and analyze cancer genomics data from the NCI GDC.
Query gene-disease validity data and detect consensus or conflicts across assertions.
Look up ancestry-specific allele frequencies, gene constraint, variants, and coverage in gnomAD.
Search, compare, and synthesize plant genomics data across multiple sources.
Access biomedical APIs to explore genes, drugs, diseases, and clinical research.
Query GlyGen summaries for proteins, glycans, sites, biomarkers, and diseases.